Clearmind Medicine
Clearmind Medicine is a clinical-stage biotech developing non-hallucinogenic, MEAI-based psychedelic therapeutics, led by CMND-100 for Alcohol Use Disorder in FDA Phase I/IIa trials, with pipeline expansion into obesity, depression, PTSD, and binge behavior disorders.
- Company typePublic
- Founded2015
- HeadquartersVancouver, Canada
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What Clearmind Medicine does
Clearmind Medicine is a clinical-stage pharmaceutical biotech developing non-hallucinogenic, psychedelic-derived therapeutics based on its proprietary molecule MEAI (5-methoxy-2-aminoindane). The company's lead candidate, CMND-100, is an oral drug in FDA-regulated Phase I/IIa trials for Alcohol Use Disorder (AUD), with dosing completed across all 24 participants in 4 cohorts at Yale School of Medicine, Johns Hopkins, Tel Aviv Sourasky Medical Center, and Hadassah Medical Center. The company's mechanism targets 5-HT1A receptors to produce an alcohol-like euphoric experience while signaling satiety, positioning it as a 'binge-mitigating agent' that could address AUD, binge eating, gambling, and other impulse-control disorders.
Clearmind is pursuing an expanding indication strategy through preclinical programs combining MEAI with tirzepatide (with Yissum/Hebrew University) for obesity and metabolic dysfunction-associated steatotic liver disease, and with Palmitoylethanolamide (with NeuroThera Labs/SciSparc) for binge behavior and metabolic indications. The intellectual property portfolio comprises 32 granted patents across 19 patent families spanning the US, Europe, India, China, Hong Kong, Japan, South Korea, Mexico, and Australia, with additional filings in depression and PTSD. A February 2026 development agreement with Polyrizon extends the product surface into intranasal delivery.
The company is pre-revenue and headquartered in Vancouver, Canada with operational offices in Tel Aviv, Israel. It is publicly listed on NASDAQ (CMND), the Frankfurt Stock Exchange (CWY0), and the Canadian Securities Exchange (CMND), employs 11-50 staff, and is led by CEO Dr. Adi Zuloff-Shani. The revenue model is contingent on future FDA approval of CMND-100, after which Clearmind intends to commercialize via prescription drug sales targeting patients with AUD and other indications, and to monetize its patent estate through licensing agreements with larger pharmaceutical companies. Cumulative funding raised to date includes approximately $8.15M in equity offerings plus up to $10M in committed convertible-note financing, with market capitalization of roughly $2.5M as of May 2026 following two reverse stock splits.
Clearmind Medicine firmographics
Firmographics- Name
- Clearmind Medicine
- Legal name
- Clearmind Medicine Inc.
- Website
- https://clearmindmedicine.com
- Company type
- Public
- Founded year
- 2015
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Clearmind Medicine is a clinical-stage biotech developing non-hallucinogenic, MEAI-based psychedelic therapeutics, led by CMND-100 for Alcohol Use Disorder in FDA Phase I/IIa trials, with pipeline expansion into obesity, depression, PTSD, and binge behavior disorders.
- Ownership category
- akta.pro rank
Clearmind Medicine industry classification
Industry- Product category
- Psychedelic Pharmaceuticals / Biotech Therapeutics
- NAICS
- Pharmaceutical and Medicine Manufacturing (3254)
- SIC
- Medicinal Chemicals & Botanical Products (2833)
- akta.pro primary industry
- Neurology & Psychiatry (CNS) Pharmaceuticals (HLAIAAAF)
- akta.pro secondary industry
- Neurology & CNS Specialty Pharmaceuticals (HLAIACAC)
Keywords
Where Clearmind Medicine is headquartered
LocationHeadquarters
- HQ city
- Vancouver
- HQ country
- Canada
- HQ region
- North America
Offices2 records
Markets served
Clearmind Medicine business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales
Revenue model
- Pharmaceutical Product Sales: Pre-revenue clinical-stage biotech. Once CMND-100 receives regulatory approval (FDA), the company intends to commercialize its proprietary drug candidates as regulated medicines. Revenue would come from prescription drug sales targeting patients with Alcohol Use Disorder and other indications.
- Licensing Royalties: The company may pursue licensing agreements with larger pharmaceutical companies for the development and commercialization of its proprietary compounds and patent portfolio in various jurisdictions and therapeutic indications.
Go-to-market motion1 record
Distribution channels2 records
Marketing channels7 records
Clearmind Medicine product offering
Product offeringCore offering
Clearmind Medicine is a clinical-stage biotech developing proprietary non-hallucinogenic psychedelic-derived therapeutics based on its novel molecule MEAI (5-methoxy-2-aminoindane). Its lead candidate CMND-100 is an oral drug for Alcohol Use Disorder currently in FDA-regulated Phase I/IIa clinical trials. The company also develops MEAI-based combination therapies for obesity, metabolic disorders, depression, PTSD, and binge behavior disorders.
Product overview
Clearmind Medicine is a clinical-stage neuroplastogens pharmaceutical biotech company developing non-hallucinogenic, second-generation psychedelic-derived therapeutics. The company's primary product portfolio centers on CMND-100, a proprietary oral drug candidate based on the MEAI (5-methoxy-2-aminoindane) molecule, which is being developed primarily for Alcohol Use Disorder (AUD) treatment. The MEAI molecule acts as a 'binge-mitigating agent' that produces alcohol-like euphoria while signaling the brain that it is satisfied, reducing the desire to consume alcohol. CMND-100 is currently undergoing Phase I/IIa FDA-regulated clinical trials at leading institutions. The company is also exploring additional therapeutic applications of MEAI including depression, obesity/metabolic disorders, PTSD, and cocaine addiction. Clearmind's intellectual property portfolio consists of 19 patent families with 32 granted patents across multiple jurisdictions worldwide.
Differentiator
Problem solved
Functional benefit
Products and services
- CMND-100 Proprietary non-hallucinogenic MEAI-based oral drug candidate for treating Alcohol Use Disorder (AUD). Currently in Phase I/IIa FDA-regulated clinical trials at leading institutions including Yale School of Medicine, Johns Hopkins University, Tel Aviv Sourasky Medical Center, and Hadassah Medical Center. Demonstrated strong safety profile with no serious adverse events reported across all 24 participants in Part A.
- MEAI (5-methoxy-2-aminoindane) Proprietary psychoactive aminoindane molecule that exerts a euphoric alcohol-like experience and reduces desire to consume alcoholic beverages. Acts on neural pathways including 5-HT1A to decrease impulsivity. Active ingredient in CMND-100, being developed for multiple indications including AUD, depression, obesity, and binge behaviors.
Quantifiable outcome
- Phase I/IIa trial: All 24 participants across Cohorts 1-4 completed treatment with strong safety profile, no serious adverse events reported
- +3 more outcomes
Companies that use Clearmind Medicine
Customer profileSegments5 records
Ideal customer profiles3 records
Clearmind Medicine technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature5 records
Clearmind Medicine partnerships and signals
Strategic signalPartnerships
Seven partnerships are on record, tiered core.
- Yissum Research Development Company of Hebrew University of Jerusalemcore12-month preclinical research agreement evaluating MEAI (CMND-100) in combination with tirzepatide and as maintenance therapy following tirzepatide treatment in diet-induced obese mice. Study conducted by Professor Joseph Tam's team at Hebrew University. Builds on prior research showing MEAI achieved approximately 15-20% body weight reduction through increased energy expenditure while preserving lean mass.
- NeuroThera Labs Inc. (Subsidiary of SciSparc Ltd.)coreCollaboration on combination therapy of MEAI with Palmitoylethanolamide (PEA) targeting obesity, metabolic dysfunction-associated steatotic liver disease (MASLD), and binge behavior disorders. Collaboration has resulted in 13 patent families across multiple jurisdictions. MEAI provides neuroplastic properties while PEA offers anti-inflammatory and neuroprotective benefits.
- Polyrizon Ltd.coreDevelopment agreement to create an intranasal formulation of MEAI using Polyrizon's proprietary intranasal hydrogel technology. The partnership aims to improve bioavailability through enhanced nasal residence time and targeted delivery for CNS-targeted compounds. Classified as a related party transaction under Canadian securities regulations.
- Tel Aviv Sourasky Medical Center (TASMC)coreClinical trial site for Phase I/IIa trial of CMND-100 for Alcohol Use Disorder. Study led by Dr. David Zeltser, Director of Emergency Medicine Department. One of the leading clinical sites in Israel participating in the multinational trial.
- Hadassah-University Medical CentercoreClinical trial site for Phase I/IIa trial of CMND-100 for Alcohol Use Disorder. Led by Prof. Yossi Karko, Director of Center for Clinical Research, and Prof. Joseph Caraco, Director of Clinical Pharmacology Unit. One of the premier research institutions in Israel.
- Yale School of MedicinecoreLeading U.S. clinical trial site for Phase I/IIa trial of CMND-100. Department of Psychiatry involvement in the FDA-regulated multicenter, randomized, double-blind, placebo-controlled study.
- Johns Hopkins University School of MedicinecoreLeading U.S. clinical trial site for Phase I/IIa trial of CMND-100. Johns Hopkins Medicine Institutional Review Board approved advancement to Parts B and C of the trial. Key site for safety and tolerability evaluation.
Scale indicators8 records
Recent moves7 records
Expansion highlights7 records
Clearmind Medicine competitors and assessment
Company assessmentBroad incumbents
- Tonix Pharmaceuticals: Commercial and clinical-stage CNS-focused biopharmaceutical company with a broader neurology and psychiatry portfolio (e.g., fibromyalgia, migraine). Overlaps with Clearmind's CNS specialty pharmaceutical focus but operates across a wider set of indications.
- Axsome Therapeutics: Commercial-stage CNS biopharmaceutical company with FDA-approved Auvelity for major depressive disorder and others for migraine. Comparable as a publicly-traded CNS specialty pharma pursuing novel mechanisms in psychiatry.
- Sage Therapeutics: Established CNS biopharmaceutical company with FDA-approved Zurzuvae for postpartum depression and a pipeline targeting depression and neurological disorders. A broader incumbent in the CNS specialty pharmaceutical category where Clearmind also operates.
Direct peers
- Cybin: Clinical-stage psychedelic therapeutics company developing deuterated psilocybin analog CYB003 for depression and other mental health conditions. Comparable in size, stage, and psychedelic CNS focus.
- Compass Pathways: Late-stage psychedelic biotech developing psilocybin therapy for treatment-resistant depression. Comparable to Clearmind as a publicly-traded, FDA-regulated psychedelic therapeutics company pursuing CNS indications with proprietary novel molecules.
- GH Research: Clinical-stage company developing mebufotenin and other psychedelic-derived candidates for treatment-resistant depression. Comparable to Clearmind as a small-cap, FDA-regulated psychedelic therapeutics developer focused on CNS indications.
- atai Life Sciences: Clinical-stage biopharmaceutical platform developing psychedelic and non-psychedelic therapeutics for mental health, including depression and addiction. Closely comparable to Clearmind in psychedelic-derived CNS pipeline strategy.
- MindMed: Clinical-stage psychedelic medicine biotech developing candidates for anxiety, ADHD, and substance use disorders. Directly comparable to Clearmind as a public, CNS-focused psychedelic-derived therapeutics developer with overlapping addiction indications.
Emerging players
- NeuroThera Labs (SciSparc): Specialty pharmaceutical company developing cannabinoid-based therapies for CNS indications, including a collaboration with Clearmind on MEAI+PEA combinations. Directly involved as a partner and represents a peer in CNS combination therapeutics.
- Bionomics Limited: Clinical-stage CNS biopharmaceutical company developing BNC210 for anxiety and PTSD. Comparable as a small-cap CNS-focused emerging player targeting overlapping mental health indications.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks6 records
Key highlights7 records
Customer concentration
Clearmind Medicine social profiles
Digital presenceClearmind Medicine compliance and trust
Trust signalCompliance1 record
Clearmind Medicine financial estimates
Financial estimateRevenue estimate
Valuation estimate
Clearmind Medicine leadership team
Management profileNumber of profiles
Profiles12 records
Clearmind Medicine funding detail
Funding detailFunding overview
Funding rounds4 records
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Clearmind Medicine M&A and investment
M&A and investmentM&A1 record
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Clearmind Medicine
What does Clearmind Medicine do?
Clearmind Medicine is a clinical-stage biotech developing proprietary non-hallucinogenic psychedelic-derived therapeutics based on its novel molecule MEAI (5-methoxy-2-aminoindane). Its lead candidate CMND-100 is an oral drug for Alcohol Use Disorder currently in FDA-regulated Phase I/IIa clinical trials. The company also develops MEAI-based combination therapies for obesity, metabolic disorders, depression, PTSD, and binge behavior disorders.
Is Clearmind Medicine a public or private company?
Clearmind Medicine is a public company. It is classified as public and is currently operating.
When was Clearmind Medicine founded?
Clearmind Medicine was founded in 2015. It employs 11 to 50 people.
Where is Clearmind Medicine based?
Clearmind Medicine is headquartered in Vancouver, Canada, in the North America region.
How does Clearmind Medicine make money?
Two revenue lines are on record. Pharmaceutical Product Sales are the primary driver. The others are licensing Royalties.
Who are Clearmind Medicine's main competitors?
Broad incumbents on record are Tonix Pharmaceuticals, Axsome Therapeutics and Sage Therapeutics. Direct peers are Cybin, Compass Pathways, GH Research, atai Life Sciences and MindMed. Emerging players are NeuroThera Labs (SciSparc) and Bionomics Limited.
Does Clearmind Medicine have an API?
No public API is recorded for Clearmind Medicine.
What industry is Clearmind Medicine in?
Clearmind Medicine's product category is Psychedelic Pharmaceuticals / Biotech Therapeutics. Its primary akta.pro industry code is HLAIAAAF, Neurology & Psychiatry (CNS) Pharmaceuticals, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 3254 and its SIC code is 2833.